Canonical Allele Identifier: CA2057673617
Gene: TMPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98534333T= , CM000674.2:g.98534333T= GRCh38
NC_000012.11:g.98928111T= , CM000674.1:g.98928111T= GRCh37
NC_000012.10:g.97452242T= NCBI36
NG_021393.1:g.23761T= , LRG_443:g.23761T=

Transcript Alleles

HGVS Amino-acid change
ENST00000556029.6:c.565+2495T= MANE Select ENSP00000450627.1:n.565+2495T=
ENST00000261210.9:c.565+2495T= ENSP00000261210.5:n.565+2495T=
ENST00000266732.8:c.2076T= ENSP00000266732.4:p.Asn692=
ENST00000343315.9:c.565+2495T= ENSP00000340251.5:n.565+2495T=
ENST00000393053.6:c.565+2495T= ENSP00000376773.2:n.565+2495T=
ENST00000552831.1:n.643+2495T=
ENST00000556029.5:c.565+2495T= ENSP00000450627.1:n.565+2495T=
ENST00000556678.1:c.286+2495T= ENSP00000451552.1:n.286+2495T=
NM_001032283.2:c.565+2495T= , LRG_443t1:c.565+2495T= NP_001027454.1:n.565+2495T=
NM_001032284.2:c.565+2495T= NP_001027455.1:n.565+2495T=
NM_001307975.1:c.565+2495T= NP_001294904.1:n.565+2495T=
NM_003276.2:c.2076T= , LRG_443t2:c.2076T= NP_003267.1:p.Asn692=
XM_005269132.2:c.565+2495T= XP_005269189.1:n.565+2495T=
XM_005269132.4:c.565+2495T= XP_005269189.1:n.565+2495T=
XM_017019914.2:c.1170T= XP_016875403.1:p.Asn390=
NM_001032283.3:c.565+2495T= MANE Select NP_001027454.1:n.565+2495T=
NM_001032284.3:c.565+2495T= NP_001027455.1:n.565+2495T=
NM_001307975.2:c.565+2495T= NP_001294904.1:n.565+2495T=